Medical Device Recalls
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1 result found
510(K) Number: K103318 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Model 731 EMV+ Uni-Vent, Impact Instrumentation Inc., 27 Fairfield Place, West Caldwell NJ 07006. In... | 3 | 08/07/2012 |
FEI # 1220908 Impact Instrumentation, Inc. |
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